Canonical Allele Identifier: CA2308284657

Gene: TNFRSF11A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62359864G= , CM000680.2:g.62359864G=	GRCh38
NC_000018.9:g.60027097G= , CM000680.1:g.60027097G=	GRCh37
NC_000018.8:g.58178077G=	NCBI36
NG_008098.1:g.39550G= , LRG_194:g.39550G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586569.3:c.522-91G= MANE Select	ENSP00000465500.1:n.522-91G=
ENST00000639222.1:c.522-91G=	ENSP00000492422.1:n.522-91G=
ENST00000269485.11:c.522-91G=	ENSP00000269485.7:n.522-91G=
ENST00000586569.2:c.522-91G=	ENSP00000465500.1:n.522-91G=
ENST00000587697.1:n.440-91G=
ENST00000616710.4:c.522-91G=	ENSP00000479567.1:n.522-91G=
ENST00000617039.4:c.522-91G=	ENSP00000482466.1:n.522-91G=
NM_001270949.1:c.522-91G=	NP_001257878.1:n.522-91G=
NM_001270950.1:c.522-91G=	NP_001257879.1:n.522-91G=
NM_001270951.1:c.522-91G=	NP_001257880.1:n.522-91G=
NM_001278268.1:c.480-91G=	NP_001265197.1:n.480-91G=
NM_003839.3:c.522-91G=	NP_003830.1:n.522-91G=
XM_011526244.1:c.537-91G=	XP_011524546.1:n.537-91G=
XM_011526245.1:c.414-91G=	XP_011524547.1:n.414-91G=
XR_935263.1:n.552-91G=
XM_011526244.2:c.537-91G=	XP_011524546.1:n.537-91G=
XM_011526245.2:c.414-91G=	XP_011524547.1:n.414-91G=
XM_017026064.1:c.414-91G=	XP_016881553.1:n.414-91G=
XM_017026065.1:c.372-91G=	XP_016881554.1:n.372-91G=
XM_017026066.1:c.312-91G=	XP_016881555.1:n.312-91G=
NM_003839.4:c.522-91G= MANE Select	NP_003830.1:n.522-91G=
NM_001270951.2:c.522-91G=	NP_001257880.1:n.522-91G=
NM_001278268.2:c.480-91G=	NP_001265197.1:n.480-91G=
NM_001270949.2:c.522-91G=	NP_001257878.1:n.522-91G=
NM_001270950.2:c.522-91G=	NP_001257879.1:n.522-91G=